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与小脑扁桃体下疝畸形I型相关的脊髓空洞症的病理生理学。对诊断和治疗的启示。

Pathophysiology of syringomyelia associated with Chiari I malformation of the cerebellar tonsils. Implications for diagnosis and treatment.

作者信息

Oldfield E H, Muraszko K, Shawker T H, Patronas N J

机构信息

Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland.

出版信息

J Neurosurg. 1994 Jan;80(1):3-15. doi: 10.3171/jns.1994.80.1.0003.

Abstract

The mechanisms previously proposed for the progression of syringomyelia associated with Chiari I malformation of the cerebellar tonsils are controversial, leave many clinical observations unexplained, and underlie the prevalence of different operations currently used as initial treatment. To explore the mechanism of syringomyelia progression in this setting, the authors used anatomical and dynamic (phase-contrast and phase-contrast cine) magnetic resonance (MR) imaging, and intraoperative ultrasonography to examine the anatomy and dynamics of movement of the cerebellar tonsils, the wall of the spinal cord surrounding the syrinx, and the movement of cerebrospinal fluid (CSF) and syrinx fluid at rest, during the respiratory and cardiac cycles, and during Valsalva maneuver in seven affected patients. In all patients the cerebellar tonsils occluded the subarachnoid space at the level of the foramen magnum. Syringomyelia extended from the cervical to the lower thoracic segment of the spinal cord. No patient had evidence of a patent communication between the fourth ventricle and the syrinx on anatomical MR images, dynamic MR images, or intraoperative ultrasound studies. Dynamic MR images of three patients revealed abrupt downward movement of the spinal CSF and the syrinx fluid during systole and upward movement during diastole, but limited movement of CSF across the foramen magnum during the cardiac cycle. Intraoperative ultrasound studies demonstrated abrupt downward movement of the cerebellar tonsils during systole that was synchronous with sudden constriction of the spinal cord and syrinx. Decompression of the foramen magnum was achieved via suboccipital craniectomy, laminectomy of C-1 and C-2, and dural grafting, leaving the arachnoid intact. Immediately after surgery, the pulsatile downward thrust of the tonsils and constriction of the spinal cord and syrinx disappeared. Syringomyelia resolved within 1 to 6 months after surgery in all patients. Observations by the authors suggest the following previously unrecognized mechanism for progression of syringomyelia associated with occlusion of the subarachnoid space at the foramen magnum. The brain expands as it fills with blood during systole, imparting a systolic pressure wave to the intracranial CSF that is accommodated in normal subjects by sudden movement of CSF from the basal cisterns to the upper portion of the spinal canal. With obstruction to rapid movement of CSF at the foramen magnum, the cerebellar tonsils, which plug the subarachnoid space posteriorly, move downward with each systolic pulse, acting as a piston on the partially isolated spinal CSF and producing a systolic pressure wave in the spinal CSF that acts on the surface of the spinal cord.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

先前提出的与小脑扁桃体Chiari I畸形相关的脊髓空洞症进展机制存在争议,许多临床观察结果无法得到解释,这也是目前用作初始治疗的不同手术普遍存在的原因。为了探究这种情况下脊髓空洞症进展的机制,作者使用解剖学和动态(相位对比和相位对比电影)磁共振(MR)成像以及术中超声检查,来研究7例受影响患者的小脑扁桃体、脊髓空洞周围脊髓壁的解剖结构和运动动态,以及静息状态下、呼吸和心动周期期间以及瓦尔萨尔瓦动作时脑脊液(CSF)和脊髓空洞内液体的运动情况。在所有患者中,小脑扁桃体在枕骨大孔水平阻塞了蛛网膜下腔。脊髓空洞症从脊髓颈段延伸至胸下段。在解剖学MR图像、动态MR图像或术中超声检查中,没有患者有第四脑室与脊髓空洞之间存在通畅连通的证据。3例患者的动态MR图像显示,收缩期脊髓CSF和脊髓空洞内液体突然向下移动,舒张期向上移动,但心动周期期间CSF通过枕骨大孔的移动有限。术中超声检查显示,收缩期小脑扁桃体突然向下移动,与脊髓和脊髓空洞的突然收缩同步。通过枕下颅骨切除术、C-1和C-2椎板切除术以及硬脑膜移植实现枕骨大孔减压,保留蛛网膜完整。手术后立即,扁桃体的搏动性向下推力以及脊髓和脊髓空洞的收缩消失。所有患者的脊髓空洞症在术后1至6个月内消退。作者的观察结果提示了以下先前未被认识到的与枕骨大孔蛛网膜下腔阻塞相关的脊髓空洞症进展机制。心脏收缩期大脑充血时会扩张,将收缩期压力波传递给颅内CSF,在正常受试者中,CSF会通过从基底池突然移动到椎管上部来适应这种情况。由于枕骨大孔处CSF快速移动受阻,向后堵塞蛛网膜下腔的小脑扁桃体随着每次收缩期脉冲向下移动,就像一个活塞作用于部分隔离的脊髓CSF,并在脊髓CSF中产生一个作用于脊髓表面的收缩期压力波。(摘要截取自400字)

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